Segregation of Nitrogen Fixation and Oxygenic Photosynthesis in the Marine Cyanobacterium Trichodesmium

Author:

Berman-Frank Ilana1,Lundgren Pernilla2,Chen Yi-Bu1,Küpper Hendrik345,Kolber Zbigniew1,Bergman Birgitta2,Falkowski Paul1

Affiliation:

1. Environmental Biophysics and Molecular Ecology Program, Institute of Marine and Coastal Sciences, Rutgers University, 71 Dudley Road, New Brunswick, NJ 08901, USA.

2. Department of Botany, Stockholm University, SE–106 91 Stockholm, Sweden.

3. Photosynthesis Research Center, Institute of Microbiology, Opatovickýmlýn, CZ–37981 Třeboň, Czech Republic.

4. Laboratory of Biomembranes, University of South Bohemia, Branišovská 31, CZ–370 05 ČeskéBudějovice, Czech Republic.

5. University of Konstanz, Faculty of Sciences, Department of Biology, D–78457 Konstanz, Germany.

Abstract

In the modern ocean, a significant amount of nitrogen fixation is attributed to filamentous, nonheterocystous cyanobacteria of the genus Trichodesmium. In these organisms, nitrogen fixation is confined to the photoperiod and occurs simultaneously with oxygenic photosynthesis. Nitrogenase, the enzyme responsible for biological N 2 fixation, is irreversibly inhibited by oxygen in vitro. How nitrogenase is protected from damage by photosynthetically produced O 2 was once an enigma. Using fast repetition rate fluorometry and fluorescence kinetic microscopy, we show that there is both temporal and spatial segregation of N 2 fixation and photosynthesis within the photoperiod. Linear photosynthetic electron transport protects nitrogenase by reducing photosynthetically evolved O 2 in photosystem I (PSI). We postulate that in the early evolutionary phase of oxygenic photosynthesis, nitrogenase served as an electron acceptor for anaerobic heterotrophic metabolism and that PSI was favored by selection because it provided a micro-anaerobic environment for N 2 fixation in cyanobacteria.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference54 articles.

1. P. W. Ludden G. P. Roberts in Anoxygenic Photosynthetic Bacteria R. E. Blankenship M. T. Madigan C. E. Bauer Eds. (Kluwer Academic Dordrecht Netherlands 1995) pp. 929–947.

2. In cyanobacteria nitrogenase consists of two proteins: the iron protein and the iron-molybdenum protein. The former is an α 2 dimer with a molecular weight (MW) of about 65 000 that contains a single Fe 4 S 4 cluster bound between subunits. The latter is an α 2 β 2 heterotetramer of approximate MW of 250 000 with each unit containing two types of clusters the P cluster and the FeMoco center (sometimes called the M cluster). The P cluster is an Fe 8 S 7 center that functions as a conduit for electron transfer accepting electrons from the Fe 4 S 4 cluster of the iron protein [in conjunction with adenosine triphosphate (ATP) hydrolysis] and donating them to the FeMoco center which is the site of N 2 reduction. Whereas both the Fe 4 S 4 and P clusters are inactivated by O 2 the Fe 4 S 4 cluster is much more susceptible and irreversibly damaged (34).

3. R. C. Dugdale et al. Deep Sea Res. 7 297 (1961).

4. Diel variation in nitrogen fixation by a marine blue-green alga, Trichodesmium thiebautii

5. Marine Oscillatoria ( Trichodesmium ): Explanation for Aerobic Nitrogen Fixation Without Heterocysts

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